Onium borates/borates of organometallic complexes and cationic initiation of polymerization therewith

ABSTRACT

Novel onium borates of an element of Groups 15 to 17 of the Periodic Table, or borates of an organometallic complex of an element of Groups 4 to 10 of the Periodic Table, well suited for the photochemical/electron beam cationic initiation of polymerization/crosslinking, the anionic borate moiety of which having the formula: 
     
         [BX.sub.a R.sub.b ].sup.- 
    
     in which a and b are integers ranging from 0 to 4 and a+b=4; the symbols X are each a halogen atom when a ranges up to 3 and an OH functional group when a ranges up to 2; and the symbols R, which may be identical or different, are each a phenyl radical substituted by at least one element or electron-withdrawing substituent or by at least two halogen atoms, or an aryl radical containing at least two aromatic ring members, or such aryl radical bearing at least one electron-withdrawing substituent.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of application Ser. No. 08/634,228 filed on Apr. 18, 1996 (now U.S. Pat. No. 5,668,192), which is a divisional of application Ser. No. 08/400,970 filed on Mar. 8, 1995 (now U.S. Pat. No. 5,550,265), which is a divisional of application Ser. No. 08/035,838 filed on Mar. 23, 1993 (now U.S. Pat. No. 5,468,902).

This application also claims priority to application Ser. No. 92/03440 filed on Mar. 23, 1992 in France under 35 U.S.C. § 119; the content of which is hereby incorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to novel onium borates or borates of organometallic complexes which are cationic initiators of polymerization, to a process for the preparation thereof and to the use of such novel borates for the polymerization or crosslinking of functional polymers, oligomers or monomers by photochemical activation, or activation under an electron beam.

2. Description of the Prior Art

Onium salts or salts of organometallic complexes are well known to this art as initiators of the cationic polymerization of monomers or of polymers substituted by functional groups of the epoxy or vinyl ether type, or the like (U.S. Pat. Nos. 4,069,054; 4,450,360; 4,576,999 and 4,640,967; Canadian Patent No. 1,274,646; European Application EP-A-203,829).

It has been observed that the best results are obtained when the anion of the initiator salt is SbF₆ ⁻ ; the initiator salts containing this type of anion, however, present toxicity risks.

It is also known to this art to use ferrocenium perfluorotetraphenylborates of the bis(η⁵ -cyclopentadienyl)Fe⁺ tetrakis(pentafluorophenyl)borate type for generating catalysts of the Ziegler-Natta variety, which catalysts are then used for polymerizing vinyl monomers (EP-A-481,480; EP-A-468,651; EP-A-418,044; EP-A-468,537; EP-A-421,659 and EP-A-277,044; Makromol. Chem., Rapid Commun., 12, 663-667 (1991); Organometallics, 10, 840-842 (1991); it has been observed that the ferrocenium perfluorotetraphenylborates of the bis(η⁵ -cyclopentadienyl)Fe⁺ tetrakis(pentafluorophenyl)borate type are not photoinitiators.

SUMMARY OF THE INVENTION

Novel such photoinitiator salts have now been found containing an anion with a nucleophilicity close to that of SbF₆ ⁻ but which does not present the disadvantages thereof.

Briefly, the present invention features onium borates of an element from Groups 15 to 17 of the Periodic Table [Chem. & Eng. News, Vol. 63, No. 5, 26; Feb. 4, 1985] or borates of an organometallic complex of an element from Groups 4 to 10 of the Periodic Table (same reference), the cationic moiety of which comprising:

(1) an onium salt having the formula (I):

    [(R.sup.1).sub.n --A--(R.sup.2).sub.m ].sup.+              (I)

in which A is an element from Groups 15 to 17 of the Periodic Table, such as I, S, Se, P, N and the like; R¹ is a C₆ -C₂₀ heterocyclic or carbocyclic aryl radical, said heterocyclic radical containing at least one of the heteroatoms, nitrogen, sulfur, and the like; R² is R¹ or a linear or branched, C₁ -C₃₀ alkenyl or alkyl radical, said radicals R¹ and R² optionally being substituted by a C₁ -C₂₅ alkoxy, C₁ -C₂₅ alkyl, nitro, chloro, bromo, cyano, carboxyl, ester, mercapto group and the like; n is an integer ranging from 1 to v+1, with v being the valence of the element A; and m is an integer ranging from 0 to v-1 with n+m=v+1;

(2) an oxoisothiochromanium salt as described in WO-A-90/11,303, especially the 2-ethyl-4-oxoisothiochromanium or 2-dodecyl-4-oxoisothiochromanium sulfonium salt; or

(3) an organometallic salt having the formula (II):

    (L.sup.1 L.sup.2 L.sup.3 M).sup.q+                         (II)

in which M is a metal from Groups 4 to 10 of the Periodic Table, especially iron, manganese, chromium, cobalt, and the like; L¹ is one ligand joined to the metal M via π electrons, said ligand being selected from among the η³ -alkyl, η⁵ -cyclopentadienyl and η⁷ -cycloheptatrienyl ligands and the η⁶ -aromatic compounds selected from among the optionally substituted η⁶ -benzene ligands and the compounds having from 2 to 4 condensed rings, each ring being capable of contributing to the valence shell of the metal M via 3 to 8 π electrons; L² is one ligand joined to the metal M via π electrons, said ligand being selected from among the η⁷ -cycloheptatrienyl ligands and the η⁶ -aromatic compounds selected from among the optionally substituted η⁶ -benzene ligands and the compounds having from 2 to 4 condensed rings, each ring being capable of contributing to the valence shell of the metal M via 6 or 7 π electrons; L³ is from 0 to 3 identical or different ligands joined to the metal M via σ electrons, said ligand(s) being selected from among CO and NO₂ ⁺, with the proviso that the total electron charge q of the complex to which L¹, L² and L³ contribute and the ionic charge of the metal M are positive and equal to 1 or 2; and the anionic borate moiety of which having the formula:

    [BX.sub.a R.sub.b ].sup.-

in which a and b are integers ranging from 0 to 4 with a+b=4; each X is a halogen atom (chlorine or fluorine) with a=0 to 3, an OH functional group with a=0 to 2; the symbols R, which may be identical or different, are each a phenyl radical substituted by at least one electron-withdrawing group, such as CF₃, NO₂, CN and the like, or by at least two halogen atoms (most particularly fluorine), (with the proviso that the cationic moiety is an onium of an element from Groups 15 to 17 of the Periodic Table); or are each a phenyl radical substituted by at least one element or one electron-withdrawing group, especially a halogen atom (most particularly fluorine), CF₃, NO₂, CN and the like, with the proviso that the cationic moiety is an organometallic complex of an element from Groups 4 to 10 of the Periodic Table; or are each an aryl radical containing at least two aromatic ring members, such as biphenyl, napthyl and the like, optionally substituted by at least one element or one electron-withdrawing group, especially a halogen atom (most particularly fluorine), CF₃, NO₂, CN and the like, whatever the cationic moiety.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS OF THE INVENTION

More particularly according to the present invention, exemplary borate anions include:

[B(C₆ F₅)₄ ]⁻, [B(C₆ H₄ CF₃)₄ ]⁻, [(C₆ F₅)₂ BF₂ ]⁻, [C₆ F₅ BF₃ ]⁻, [B(C₆ H₃ F₂)₄ ]⁻.

The onium salts of formula (I) are described in the literature, patent and otherwise, and especially in U.S. Pat. Nos. 4,026,705; 4,032,673; 4,069,056; 4,136,102 and 4,173,476, for example.

The following cations, wherein Φ is phenyl, are very particularly representative:

[(Φ)₂ I]⁺, [C₈ H₁₇ --O-Φ-I-Φ]⁺, [C₁₂ H₂₅ -Φ-I-Φ]⁺, [(C₈ H₁₇ --O-Φ)₂ I]⁺, [(C₈ H₁₇)--O-Φ-I-Φ]⁺, [(Φ)₃ S]⁺, [(Φ₂ -S-Φ-O--C₈ H₁₇ ]⁺, [Φ-S-Φ-S(Φ)₂ ]⁺, [(C₁₂ H₂₅ -Φ)₂ I]⁺.

The organometallic salts of formula (II) appear among those described in U.S. Pat. Nos. 4,973,722 and 4,992,572 and the European Patent Applications EP-A-203,829, EP-A-323,584 and EP-A-354,181.

Exemplary of such organometallic salts, very particularly representative are:

(η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺,

(η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺,

(η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺,

Bis(η⁶ -mesithylene)Fe⁺,

Bis(η⁶ -benzene)Cr⁺.

Thus, exemplary initiators of the invention include:

[(Φ)₂ ]⁺ [B(C₆ f₅)₄ ]⁻, [c₈ H₁₇ --O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [C₁₂ H₂₅ -Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇ --O-Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇)--O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₃ S]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₂ S-Φ-O--C₈ H₁₇ ]⁺ [B(C₆ H₄ CF₃)₄ ]⁻, [C₁₂ H₂₅ -Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺ [B(C₆ F₅)₄ ]⁻.

The initiator salts of the present invention can be prepared by an exchange reaction between a salt of the cationic moiety (halide such as chloride, iodide and the like, hexafluorophosphate, tetrafluoroborate, tosylate and the like) and an alkali metal salt (sodium, lithium or potassium) of the anionic moiety.

The operating conditions (respective amounts of reactants, choice of solvents, duration, temperature, stirring and the like) are easily determined by one skilled in this art; they must permit recovery of the desired initiator salt in the solid state, by filtration of the precipitate formed, or in the oily state by extraction using a suitable solvent.

The alkali metal salts of the anionic moiety can be prepared in known manner, by an exchange reaction between a haloborated compound and an organometallic compound (of magnesium, lithium, tin and the like) bearing the desired hydrocarbon groups, in a stoichiometric amount, optionally followed by a hydrolysis using an aqueous solution of alkali metal halide; this type of synthesis is, for example, described in J. of Organometallic Chemistry, Vol. 178, p. 1-4, (1979); J.A.C.S., 82, 5298 (1960); Anal. Chem. Acta, 44, 175-183 (1969); U.S. Pat. No. 4,139,681 and DE-A-2,901,367; Zh. Org. Khim., Vol. 25, No. 5--pages 1099-1102, (May 1989).

The preparation of the salts of the cationic moiety of formula (II) is described, especially, in D. Astruc, Tetrahedron Letters, 36, p. 3437 (1973); D. Astruc, Bull. Soc. Chim. Fr., 1-2, p. 228 (1976); D. Astruc, Bull. Soc. Chim. Fr., 11-12, p. 2571 (1975); D. Astruc, CR Acad. Sc., Paris, series C, 272, p. 1337 (1971); A. N. Nesmeyanov et al, Izves. Akad. Nauk SSSR, ser. Khim., 7, p. 1524 (1969); A. N. Nesmeyanov et al., Dokl. Akad. Nauk SSSR, 160(6), p. 1327 (1965); A. N. Nesmeyanov et al, Dokl. Akad. Nauk SSSR, 149(3), p. 615 (1963).

The initiator salts of the present invention are useful for polymerizing or crosslinking, by photochemical activation (especially under ultraviolet radiation) or under an electron beam, monomers, oligomers or polymers bearing functional groups such as epoxy groups, vinyl ether groups, and the like. The borates of the organometallic complexes can additionally be used as thermal polymerization initiators.

The polymerizable and/or crosslinkable monomer(s) and/or oligomer(s) and/or polymer(s) belong(s) to at least one of the following non-organosilic compounds: cycloaliphatic epoxies (A), non-cycloaliphatic epoxies (B), linear or cyclic alkenyl ethers (C) and mixtures of A, B and/or C with one or more organic acrylic compounds (D).

The compounds A, B and C are preferably chosen from the compounds:

A: cycloaliphatic epoxies, alone or mixed with each other, including epoxies of the type 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate or bis(3,4-epoxycyclohexyl) adipate or diglycidyl 1,2-cyclohexane dicarboxylate,

B: non-cycloaliphatic epoxies, alone or mixed with each other, including:

epoxies such as those resulting from the condensation of bisphenol A or a non-aromatic polyol and epichlorhydrin such as, for example, the following di- and triglycidyl ethers: bisphenol A possibly alkoxylated, 1,6-hexanediol, glycerol, neopentylglycol and trimethylol propane,

epoxies such as those resulting from the oxidation of polyolefins such as butadiene or unsaturated fatty acids such as soybean oil or linseed oil,

C: linear or cyclic alkenyl ethers alone or mixed with each other, including:

vinyl ethers, such as: divinylglycol triethylene ether, divinyl 1,4-cyclohexanedimethanol ether, cyclic vinyl ethers or acrolein tetramers and/or dimers,

propenyl ethers,

and butenyl ethers.

Acrylic D compounds that can be mixed with A, B and/or C are preferably chosen from the compounds:

1,6-hexanediol diacrylate, trimethylolpropane triacrylate, tripropyleneglycol diacrylate, glycidylpropyl triacrylate (product SERVOCURE RM 188® marketed by the company HULS).

As used herein, the expression "acrylic" includes compounds comprising the function of the type CH₂ ═CH-- or CH₂ ═C(CH₃)--.

Other suitable polymerizable and/or crosslinkable monomer(s) and/or oligomer(s) and/or polymer(s) include those which contain at least one functional group such as cyclic ethers, vinylamines, unsaturated hydrocarbons, lactones and other cyclic esters, lactams, cyclic carbonates, cyclic acetals, aldehydes, cyclic amines, cyclic sulfides, cyclosiloxanes, cyclotriphosphazenes, and other polymerizable and/or crosslinkable groups described in G. Odian, Principles of Polymerization (3d ed. 1991) and Encyclopedia of Polymer Science and Engineering, pp. 729-814 (Mark et al. eds., 1985).

Particularly useful examples of cyclic ether monomers are described in U.S. Pat. No. 4,985,340, the content of which is hereby incorporated by reference; and examples of vinyl organic monomers are described in U.S. Pat. No. 4,264,703, the content of which is hereby incorporated by reference.

In order to further illustrate the present invention and the advantages thereof, the following specific examples are given, it being understood that some are intended only as illustrative and in nowise limitative.

EXAMPLE 1 Diphenyliodonium tetrakis (pentafluorophenyl)borate [(Φ₂ I]⁺ [B(C₆ F₅)₄ ]⁻

Preparation of lithium tetrakis(pentafluorophenyl)-borate:

A 4,000 ml, four-necked, round-bottom flask, equipped with a mechanical stirrer, a water-cooled reflux condenser, a thermometer and a dropping funnel, was employed. The assembly was dried beforehand under an argon atmosphere.

1,600 ml of anhydrous pentane and 126.8 g (or 0.513 mol) of bromopentafluorobenzene were charged therein. This medium was stirred and then cooled to -78° C. using a solid carbon dioxide/acetone bath.

313 ml of a 1.6M solution of n-butyllithium in hexane were charged into the dropping funnel and were then added dropwise over 50 minutes.

The mixture was maintained under stirring for 5 hours at a temperature of -78° C.

125 ml of a 1M solution of boron trichloride in hexane were charged into the dropping funnel and added to the mixture over thirty minutes. The cooling bath was removed and the reaction mixture was permitted to return to room temperature. It was then maintained under stirring for 12 hours. The reaction mixture was hydrolyzed by slow addition of 625 ml of water. The two phases were separated and the organic phase was washed with two 125 ml fractions of water. The aqueous phases were combined and were then extracted three times with ether (3×125 ml). The ether phases were combined and dried over magnesium sulfate. The ether was evaporated under reduced pressure and 101 g (or a yield of 99%) of lithium tetrakis(pentafluorophenyl)borate were recovered.

Preparation of diphenyliodonium tetrakis(pentafluorophenyl)borate:

7.17 g (or 22.6 mmol) of diphenyliodonium chloride were dissolved in 300 ml of water in a 1,000 ml Erlenmeyer flask. 15.52 g (or 22.6 mmol) of lithium tetrakis(pentafluorophenyl)borate in solution in 250 ml of water were added dropwise. The mixture was maintained under stirring for 30 minutes and was then filtered. The filtrate was dried under reduced pressure (133 Pa) overnight with the exclusion of light. 16.33 g (or a yield of 75%) of diphenyliodonium tetrakis(pentafluorophenyl)borate were thus recovered.

EXAMPLE 2 (4-Octyloxyphenyl)phenyliodonium tetrakis(pentafluorophenyl)borate [(C₈ H₁₇)--O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻

Preparation of octyl phenyl ether:

44.8 g (or 0.477 mol) of phenol, 38.6 g (or 0.2 mol) of n-bromooctane, 6 g of tetrabutylammonium bromide, 26.8 g of potassium hydroxide, 100 ml of water and 100 ml of toluene were charged into a 500 ml, three-necked, round-bottom flask equipped with a mechanical stirrer, a thermometer and water-cooled reflux condenser. This medium was stirred and was then heated to reflux for 20 hours. The reaction mixture was then cooled to room temperature. The phases were settled and separated. The organic phase was washed with 100 ml of a 0.5N sodium hydroxide solution and then with five 100 ml fractions of water. It was then dried over magnesium sulfate and the solvent was then driven off under reduced pressure at a temperature of 85° C.

41.5 g (or a yield of 95%) of n-octyl phenyl ether, which could be used subsequently without additional purification, were recovered.

Preparation of hydroxytosyloxyiodobenzene:

80.53 g (or 0.25 mol) of iodobenzene diacetate, 300 ml of water and 100 ml of acetic acid were charged into a 1,000 ml, round-bottom flask equipped with a mechanical stirrer, a water-cooled reflux condenser and a dropping funnel. This medium was stirred and heated to 40° C. 47.55 g (or 0.25 mol) of paratoluenesulfonic acid monohydrate were then added over five minutes via the dropping funnel. The reaction mixture was maintained at 40° C. for two hours and was then cooled to 25° C. A white precipitate appeared. It was recovered by filtration and then dried under reduced pressure.

68.15 g (or a yield of 70%) of the desired product were obtained.

Preparation of (4-octyloxyphenyl)phenyliodonium tosylate:

22.2 g (or 0.057 mol) of hydroxytosyloxyiodobenzene, 9 g (or 0.04 mol) of n-octyl phenyl ether, 5 ml of acetonitrile and 1.5 ml of acetic acid were charged into a 250 ml Erlenmeyer flask equipped with a magnetic stirrer bar. This mixture was stirred and was heated to a temperature of 40° C. for 2 hours, 30 minutes. 1.5 ml of glacial acetic acid was then added and the mixture was then maintained for 5 hours at 40° C. The reaction mixture was permitted to cool and 150 ml of water were added while stirring vigorously. This mixture was then stirred for 12 hours at room temperature and was then separated. The organic phase was washed several times with water, until a yellow precipitate appeared. This solid was recovered by filtration, was washed with 50 ml of ether and was then dried under vacuum at a temperature of 45° C.

19.5 g (or a yield of 76%) of (4-octyloxyphenyl)phenyliodonium tosylate were thus recovered.

Preparation of (4-octyloxyphenyl)phenyliodonium tetrakis(Pentafluorophenyl)borate:

5 g (or 0.0086 mol) of (4-octyloxyphenyl)-phenyliodonium tosylate were dissolved in 350 ml of acetone in a 500 ml Erlenmeyer flask equipped with a magnetic stirrer bar. While light was excluded, 3.4 g (or 0.0103 mol) of lithium tetrakis(pentafluorophenyl)borate in solution in 50 ml of acetone were added. The mixture was stirred for 48 hours and was then filtered to remove the lithium p-toluenesulfonate formed. The acetone was evaporated under reduced pressure and 7.98 g (or a yield of 92%) of ((4-octyloxyphenyl)phenyliodonium tetrakis(pentafluorophenyl)borate were recovered.

EXAMPLE 3 Bis(dodecylphenyl)iodonium tetrakis(pentafluorophenyl)borate [(C₁₂ H₂₅ -Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻

Preparation of bis(dodecylfluorophenyl)iodonium chloride:

100 g (or 0.405 mol) of dodecylbenzene, 43.5 g (or 0.203 mol) of potassium iodate, 199.6 g of acetic acid and 59.5 g of acetic anhydride were charged into a 1,000 ml, round-bottom flask equipped with a mechanical stirrer, a water-cooled reflux condenser and a dropping funnel. The mixture was stirred and then cooled in an ice bath to 0° C. A mixture of 59.8 g of sulfuric acid and 39.86 g of acetic acid was charged into the dropping funnel. This mixture was added to the reaction mixture over 25 minutes. The reaction mixture was maintained under stirring for 18 hours at room temperature. 750 ml of water were then added and the reaction mixture was then extracted with three ether fractions (3×350 mol). The ether phases were combined and then evaporated under reduced pressure. The concentrate was taken up in 540 ml of a saturated sodium chloride solution, and the mixture was then cooled in an ice bath for two hours. The product was recovered by filtration on sintered glass No. 4. The solid was then recrystallized twice from acetone. 69.18 g (or a yield of 52%) of bis(dodecylphenyl)iodonium chloride were recovered by filtration.

Preparation of bis(dodecylphenyl)iodonium tetrakis(pentafluorophenyl)borate:

3.76 g of bis(dodecylphenyl)iodonium chloride were dissolved in 500 ml of acetone in a 1,000 ml Erlenmeyer flask. A solution of 5 g of lithium tetrakis(pentafluorophenyl)borate in 100 ml of acetone was then added dropwise. The mixture was maintained under stirring for two days, with the exclusion of light, and the sodium chloride formed was then removed by filtration. 8 g (or a yield of 90%) of bis(dodecylphenyl)iodonium tetrakis(pentafluorophenyl)borate were recovered after evaporation of the acetone.

EXAMPLE 4 (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺ tetrakis(pentafluorophenyl)borate

4 g (or 0.0215 mol) of ferrocene, 7.64 g of aluminum chloride, 0.11 g of aluminum powder and 27 g of cumene were charged into a 250 ml, three-necked, round-bottom flask equipped with a mechanical stirrer, a water-cooled reflux condenser, a thermometer and a dropping funnel.

This medium was stirred and placed under an inert nitrogen atmosphere. The reaction mixture was heated over 2 hours, and then 4.04 g of titanium chloride were added dropwise. This medium was heated for 1 hour at 100° C. and the mixture was then permitted to return gradually to room temperature. The reaction mixture was poured into a mixture of 30 g of ice and 8 g of 37.5% HCl. The mixture was maintained under stirring for 30 min and 0.7 g of hydrogen peroxide was then added. This mixture was maintained under stirring for 30 min and was then filtered on a sintered glass No. 4. The liquid fraction was recovered; after settling and separation of the phases, a solution of 15.4 g of potassium tetrakis(pentafluorophenyl)borate in 800 ml of water was introduced into the aqueous phase. This mixture was maintained under stirring for 2 hours.

The precipitate was separated by filtration and was then dried under vacuum; 14.3 g (or a yield of 73%) of the desired product were obtained.

EXAMPLE 5 (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ tetrakis(pentafluorophenyl)borate

50 ml of an aqueous solution containing 3.58 g of (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ hexafluorophosphate were added to a 250 ml, three-necked, round-bottom flask containing 7 g of sodium tetrakis(pentafluorophenyl)borate dissolved in 100 ml of distilled water. The mixture was subjected for 1 hour to magnetic stirring. A clear precipitate formed which was separated by filtration and then dried under vacuum for 24 hours. 8.5 g (or a yield of 95%) of (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ tetrakis(pentafluorophenyl)borate were thus obtained.

The formula of the product obtained was confirmed by ¹ H and ¹⁹ F NMR and by mass spectrometry.

EXAMPLE 6 (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺ tetrakis(pentafluorophenyl)borate

The preparation was carried out as in Example 4, from 7 g of sodium tetrakis(pentafluorophenyl)borate and from 3.5 g of (η⁵ -cyclopentadienyl)(η⁶ -methylnaphthalene)Fe⁺ tetrafluoroborate; 8.9 g of the expected product were obtained.

The formula was confirmed by NMR analysis and by mass spectrometry.

EXAMPLE 7 Photocrosslinking of an Epoxidized Monomer to Form a Thin Layer

A bath was prepared according to the following procedure:

(i) 2 parts by weight of photoinitiator A in a 50% by weight solution in methanol were added, to

(ii) 100 parts by weight of epoxidized monomer UVR-6110® (3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate marketed by Union Carbide).

The mixture was maintained at room temperature for 30 minutes with mechanical stirring.

The mixture was then deposited (approximately 2 to 3 g/m²) on glassine paper (Sibille® 9530 marketed by Sibille) using a Mayer® No. 0 bar (marketed by Erichsen G-B).

The coated paper was passed under a U.V. lamp of the Fusion System® F 450 type (marketed by Fusion) and characterized by:

(a) a wavelength of 360 mm,

(b) an absence of electrodes,

(c) excitation by microwaves,

(d) a power of 120 W per cm irradiated.

The irradiation energy, measured with a Uvicure® cell from Eit-USA, was 0.025 J.cm⁻² after one pass under the UV lamp at a speed of 33 m/min.

The winding speed in m/min necessary for curing the layer was recorded.

The number of passages as well as the winding speeds of the paper appear in the following Table; the performance of the initiator prepared in Example 1 is compared with that of an initiator which had an equivalent cation but the anion on which was selected from those of the prior art.

It was observed that with an equivalent cation:

(1) the anion B(C₆ F₅)₄ ⁻ was as effective as the anion SbF₆ ⁻ without exhibiting the toxicity problems of the latter;

(2) the anion B(C₆ F₅)₄ ⁻ was much more active than the anions AsF₆ ⁻, PF₆ ⁻ and BF₄ ⁻ ;

(3) the anions B(C₆ F₅)₄ ⁻ and B(C₆ H₄ F)₄ ⁻ were ineffective in crosslinking the epoxidized monomer to form a thin layer.

    ______________________________________                                         Photoinitiator Number of  Winding speed                                          A Passages in m/min                                                          ______________________________________                                         (φ).sub.2 I.sup.+  B(C.sub.6 F.sub.5).sub.4.sup.-                                         1          60                                                     (φ).sub.2 I.sup.+  SbF.sub.6.sup.- 1 60                                    (φ).sub.2 I.sup.+  AsF.sub.6.sup.- 3 20                                    (φ).sub.2 I.sup.+  PF.sub.6.sup.- 4 15                                     (φ).sub.2 I.sup.+  BF.sub.4.sup.- 10  6                                    (φ).sub.2 I.sup.+  B(C.sub.6 H.sub.5).sub.4.sup.- not crosslinked 0        (φ).sub.2 I.sup.+  B(C.sub.6 H.sub.4 F).sub.4.sup.- not crosslinked                                0                                                    ______________________________________                                    

While the invention has been described in terms of various preferred embodiments, the skilled artisan will appreciate that various modifications, substitutions, omissions, and changes may be made without departing from the spirit thereof. Accordingly, it is intended that the scope of the present invention be limited solely by the scope of the following claims, including equivalents thereof. 

What is claimed is:
 1. A polymerizable or crosslinkable composition comprising:(a) at least one polymerizable or crosslinkable monomer or polymer; and (b) at least one initiator salt selected from the group consisting of onium borates and borates of an organometallic complex, the cationic moiety of which comprising:(1) an onium cation having the formula (I):

    [(R.sup.1).sub.n --A--(R.sup.2).sub.m ].sup.+              (I)

in which A is an element of Groups 15 to 17 of the Periodic Table; R¹ is a C₆ -C₂₀ heterocyclic or carbocyclic aryl radical; R² is R¹ or a linear or branched C₁ -C₃₀ alkenyl or alkyl radical, said radicals R¹ or R² optionally being substituted by at least one C₁ -C₂₅ alkoxy, C₁ -C₂₅ alkyl, nitro, chloro, bromo, cyano, carboxyl, ester or mercapto substituent; n is an integer ranging from 1 to v+1, with v being the valence of A; and m is an integer ranging from 0 to v-1, with the proviso that n+m=v+1; (2) an oxoisothiochromanium cation; or (3) an organometallic cation having the formula (II):

    (L.sup.1 L.sup.2 L.sup.3 M).sup.q+                         (II)

in which M is a metal of Groups 4 to 10 of the Periodic Table; L¹ is a ligand associated with the metal M via π electrons and is an η³ -allyl, η⁵ -cyclopentadienyl or η⁷ -cycloheptatrienyl ligand or an η⁶ -aromatic compound selected from among the optionally substituted η⁶ -benzene ligands and compounds having from 2 to 4 condensed ring members, each ring member contributing to the valence shell of the metal M via 3 to 8 π electrons; L² is a ligand associated with the metal M via π electrons and is an η⁷ -cycloheptatrienyl ligand or an η⁶ -aromatic compound selected from among the optionally substituted η⁶ -benzene ligands and compounds having from 2 to 4 condensed ring members, each ring member contributing to the valence shell of the metal M via 6 or 7 π electrons; and L³ represents from 0 to 3 identical or different ligands associated with the metal M via σ electrons and is CO or NO₂ ⁺ ligands, the total electron charge q of the complex to which L¹, L² and L³ contribute and the ionic charge of the metal M being positive and equal to 1 or 2; and the anionic borate moiety of which having the formula:

    [BX.sub.a R.sub.b ].sup.-

in which a and b are integers ranging from 0 to 4 and a+b=4; the symbols X are each a halogen atom when a ranges up to 3 and an OH functional group when a ranges up to 2; and the symbols R, which may be identical or different, are each a phenyl radical substituted by at least one electron-withdrawing substituent or by at least two halogen atoms, or an aryl radical containing at least two aromatic ring members, or such aryl radical bearing at least one electron-withdrawing substituent.
 2. The composition as defined by claim 1, wherein in said cationic moiety having the formula (I), A is I, S, Se, P or N.
 3. The composition as defined by claim 2, wherein in said anionic borate moiety, said at least one electron-withdrawing substituent is CF₃, NO₂, CN or at least one halogen atom.
 4. The composition as defined by claim 1, wherein said oxoisothiochromanium cation is 2-ethyl-4-oxoisothiochromanium or 2-dodecyl-4-oxoisothiochromanium sulfonium.
 5. The composition as defined by claim 1, wherein said anionic borate moiety has the formula [B(C₆ F₅)₄ ]⁻, [B(C₆ H₄ CF₃)₄ ]⁻, [(C₆ F₅)₂ BF₂ ]⁻, [C₆ F₅ BF₃ ]⁻ or [B (C₆ H₃ F₂)₄ ]⁻.
 6. The composition as defined by claim 1, wherein said cationic moiety has the formula [(Φ)₂ I]⁺, [C₈ H₁₇ -O-Φ-I-Φ]⁺, [C₁₂ H₂₅ -Φ-I-Φ]⁺, [(C₈ H₁₇ -O-Φ)₂ I]⁺, [(C₈ H₁₇)-O-Φ-I-Φ]⁺, [(Φ)₃ S]⁺, [(Φ₂ -S-Φ-O-C₈ H₁₇ ]⁺, [Φ-S-Φ-S(Φ)₂ ]⁺, [(C₁₂ H₂₅ -Φ)₂ I]⁺, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺, (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺, bis(η⁶ -mesithylene)Fe⁺ or bis(η⁶ -benzene)Cr⁺, in which Φ is phenyl.
 7. The composition as defined by claim 1, comprising:[(Φ)₂ I]⁺ [B(C₆ f₅)₄ ]⁻, [c₈ H₁₇ -O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [C₁₂ H₂₅ -Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇ -O-Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇)-O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₃ S]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₂ S-Φ-O-C₈ H₁₇ ]⁺ [B(C₆ H₄ CF₃)₄ ]⁻, [C₁₂ H₂₅ -Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺ [B(C₆ F₅)₄ ]⁻, or (η⁵ -cyclopentadienyl)(η⁶ -cumene) Fe⁺ [B(C₆ F₅)₄ ]⁻, in which Φ is phenyl.
 8. A polymerizable or crosslinkable composition comprising:(a) at least one polymerizable or crosslinkable oligomer; and (b) at least one initiator salt selected from onium borates and borates of an organometallic complex, the cationic moiety of which comprising:(1) an onium cation having the formula (I):

    [(R.sup.1).sub.n -A-(R.sup.2).sub.m ].sup.+                (I)

in which A is an element of Groups 15 to 17 of the Periodic Table; R¹ is a C₆ -C₂₀ heterocyclic or carbocyclic aryl radical; R² is R¹ or a linear or branched C₁ -C₃₀ alkenyl or alkyl radical, said radicals R¹ or R² optionally being substituted by at least one C₁ -C₂₅ alkoxy, C₁ -C₂₅ alkyl, nitro, chloro, bromo, cyano, carboxyl, ester or mercapto substituent; n is an integer ranging from 1 to v+1, with v being the valence of A; and m is an integer ranging from 0 to v-1, with the proviso that n+m=v+1; (2) an oxoisothiochromanium cation; or (3) an organometallic cation having the formula (II):

    (L.sup.1 L.sup.2 L.sup.3 M).sup.q+                         (II)

in which M is a metal of Groups 4 to 10 of the Periodic Table; L¹ is a ligand associated with the metal M via π electrons and is an η³ -allyl, η⁵ -cyclopentadienyl or η⁷ -cycloheptatrienyl ligand or an η⁶ -aromatic compound selected from among the optionally substituted η⁶ -benzene ligands and compounds having from 2 to 4 condensed ring members, each ring member contributing to the valence shell of the metal M via 3 to 8 π electrons; L² is a ligand associated with the metal M via π electrons and is an η⁷ -cycloheptatrienyl ligand or an η⁶ -aromatic compound selected from among the optionally substituted η⁶ -benzene ligands and compounds having from 2 to 4 condensed ring members, each ring member contributing to the valence shell of the metal M via 6 or 7 π electrons; and L³ represents from 0 to 3 identical or different ligands associated with the metal M via σ electrons and is CO or NO₂ ⁺ ligands, the total electron charge q of the complex to which L¹, L² and L³ contribute and the ionic charge of the metal M being positive and equal to 1 or 2; and the anionic borate moiety of which having the formula:

    [BX.sub.a R.sub.b ].sup.-

in which a and b are integers ranging from 0 to 4 and a+b=4; the symbols X are each a halogen atom when a ranges up to 3 and an OH functional group when a ranges up to 2; and the symbols R, which may be identical or different, are each a phenyl radical substituted by at least one electron-withdrawing substituent or by at least two halogen atoms, or an aryl radical containing at least two aromatic ring members, or such aryl radical bearing at least one electron-withdrawing substituent.
 9. The composition as defined by claim 8, wherein in said cationic moiety having the formula (I), A is I, S, Se, P or N.
 10. The composition as defined by claim 9, wherein in said anionic borate moiety, said at least one electron-withdrawing substituent is CF₃, NO₂, CN or at least one halogen atom.
 11. The composition as defined by claim 8, wherein said oxoisothiochromanium cation is 2-ethyl-4-oxoisothiochromanium or 2-dodecyl-4-oxoisothiochromanium sulfonium.
 12. The composition as defined by claim 8, wherein said anionic borate moiety has the formula [B(C₆ F₅)₄ ]⁻, [B(C₆ H₄ CF₃)₄ ]⁻, [(C₆ F₅)₂ BF₂ ]⁻, [C₆ F₅ BF₃ ]⁻ or [B(C₆ H₃ F₂)₄ ]⁻.
 13. The composition as defined by claim 8, wherein said cationic moiety has the formula [(Φ)₂ I]⁺, [C₈ H₁₇ -O-Φ-I-Φ]⁺, [C₁₂ H₂₅ -Φ-I-Φ]⁺, [(C₈ H₁₇ -O-Φ)₂ I]⁺, [(C₈ H₁₇)-O-Φ-I-Φ]⁺, [(Φ)₃ S]⁺, [(Φ₂ -S-Φ-O-C₈ H₁₇ ]⁺, [Φ-S-Φ-S(Φ)₂ ]⁺, [(C₁₂ H₂₅ -Φ)₂ I]⁺, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺, (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺, bis(η⁶ -mesithylene)Fe⁺ or bis(η⁶ -benzene)Cr⁺, in which Φ is phenyl.
 14. The composition as defined by claim 8, comprising: [(Φ)₂ I]⁺ [B(C₆ f₅)₄ ]⁻, [c₈ H₁₇ -O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [C₁₂ H₂₅ -Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇ -O-Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇)-O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₃ S]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₂ S-Φ-O-C₈ H₁₇ ]⁺ [B(C₆ H₄ CF₃)₄ ]⁻, [C₁₂ H₂₅ -Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺ [B(C₆ F₅)₄ ]⁻, or (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺ [B(C₆ F₅)₄ ]⁻, in which Φ is phenyl.
 15. The composition as defined by claim 8, wherein said at least one polymerizable or crosslinkable oligomer comprises at least one functional group selected from epoxies, vinyl ethers, cyclic ethers, vinylamines, unsaturated hydrocarbons, lactones and other cyclic esters, lactams, cyclic carbonates, cyclic acetals, aldehydes, cyclic amines, cyclic sulfides, cyclosiloxanes, and cyclotriphosphazenes.
 16. The composition as defined by claim 8, wherein said at least one polymerizable or crosslinkable oligomer belongs to at least one of the following groups: cycloaliphatic epoxies (A), non-cycloaliphatic epoxies (B), linear or cyclic alkenyl ethers (C) and mixtures of (A), (B), and/or (C) with at least one acrylic compound (D).
 17. A composition which is polymerizable or crosslinkable by photochemical activation or activation under an electron beam, said composition comprising:(a) at least one oligomer bearing functional group(s); and (b) at least one initiator salt selected from onium borates and borates of an organometallic complex, the cationic moiety of which comprising:(1) an onium cation having the formula (I):

    [(R.sup.1).sub.n -A-(R.sup.2).sub.m ].sup.+                (I)

in which A is an element of Groups 15 to 17 of the Periodic Table; R¹ is a C₆ -C₂₀ heterocyclic or carbocyclic aryl radical; R² is R¹ or a linear or branched C₁ -C₃₀ alkenyl or alkyl radical, said radicals R¹ or R² optionally being substituted by at least one C₁ -C₂₅ alkoxy, C₁ -C₂₅ alkyl, nitro, chloro, bromo, cyano, carboxyl, ester or mercapto substituent; n is an integer ranging from 1 to v+1, with v being the valence of A; and m is an integer ranging from 0 to v-1, with the proviso that n+m=v+1; (2) an oxoisothiochromanium cation; or (3) an organometallic cation having the formula (II):

    (L.sup.1 L.sup.2 L.sup.3 M).sup.q+                         (II)

in which M is a metal of Groups 4 to 10 of the Periodic Table; L¹ is a ligand associated with the metal M via π electrons and is an η³ -allyl, η⁵ -cyclopentadienyl or η⁷ -cycloheptatrienyl ligand or an η⁶ -aromatic compound selected from among the optionally substituted η⁶ -benzene ligands and compounds having from 2 to 4 condensed ring members, each ring member contributing to the valence shell of the metal M via 3 to 8 π electrons; L² is a ligand associated with the metal M via π electrons and is an η⁷ -cycloheptatrienyl ligand or an η⁶ -aromatic compound selected from among the optionally substituted η⁶ -benzene ligands and compounds having from 2 to 4 condensed ring members, each ring member contributing to the valence shell of the metal M via 6 or 7 π electrons; and L³ represents from 0 to 3 identical or different ligands associated with the metal M via σ electrons and is CO or NO₂ ⁺ ligands, the total electron charge q of the complex to which L¹, L² and L³ contribute and the ionic charge of the metal M being positive and equal to 1 or 2; and the anionic borate moiety of which having the formula:

    [BX.sub.a R.sub.b ].sup.-

in which a and b are integers ranging from 0 to 4 and a+b=4; the symbols X are each a halogen atom when a ranges up to 3 and an OH functional group when a ranges up to 2; and the symbols R, which may be identical or different, are each a phenyl radical substituted by at least one electron-withdrawing substituent or by at least two halogen atoms, or an aryl radical containing at least two aromatic ring members, or such aryl radical bearing at least one electron-withdrawing substituent.
 18. The composition as defined by claim 17, wherein in said cationic moiety having the formula (I), A is I, S, Se, P or N.
 19. The composition as defined by claim 18, wherein in said anionic borate moiety, said at least one electron-withdrawing substituent is CF₃, NO₂, CN or at least one halogen atom.
 20. The composition as defined by claim 17, wherein said oxoisothiochromanium cation is 2-ethyl-4-oxoisothiochromanium or 2-dodecyl-4-oxoisothiochromanium sulfonium.
 21. The composition as defined by claim 17, wherein said anionic borate moiety has the formula [B(C₆ F₅)₄ ]⁻, [B(C₆ H₄ CF₂)₄ ]⁻, [(C₆ F₅)₂ BF₂ ]⁻, [C₆ F₅ BF₃ ]⁻ or [B(C₆ H₃ F₂)₄ ]⁻.
 22. The composition as defined by claim 17, wherein said cationic moiety has the formula [(Φ)₂ I]⁺, [C₈ H₁₇ -O-Φ-I-Φ]⁺, [C₁₂ H₂₅ -Φ-I-Φ]⁺, [(C₈ H₁₇ -O-Φ)₂ I]⁺, [(C₈ H₁₇)-O-Φ-I-Φ]⁺, [(Φ)₃ S]⁺, [(Φ₂ -S-Φ-O-C₈ H₁₇ ]⁺, [Φ-S-Φ-S(Φ)₂ ]⁺, [(C₁₂ H₂₅ -Φ)₂ I]⁺, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺, (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺, bis(η⁶ -mesithylene)Fe⁺ or bis(η⁶ -benzene)Cr⁺, in which Φ is phenyl.
 23. The composition as defined by claim 17, comprising: [(Φ)₂ I]⁺ [B(C₆ f₅)₄ ]⁻, [c₈ H₁₇ -O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [C₁₂ H₂₅ -Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇ -O-Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, [(C₈ H₁₇)-O-Φ-I-Φ]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₃ S]⁺ [B(C₆ F₅)₄ ]⁻, [(Φ)₂ S-Φ-O-C₈ H₁₇ ]⁺ [B(C₆ H₄ CF₃)₄ ]⁻, [C₁₂ H₂₅ -Φ)₂ I]⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -toluene)Fe⁺ [B(C₆ F₅)₄ ]⁻, (η⁵ -cyclopentadienyl)(η⁶ -1-methylnaphthalene)Fe⁺ [B(C₆ F₅)₄ ]⁻, or (η⁵ -cyclopentadienyl)(η⁶ -cumene)Fe⁺ [B(C₆ F₅)₄ ]⁻, in which Φ is phenyl.
 24. The composition as defined by claim 17, wherein said functional group(s) is or are selected from epoxies, vinyl ethers, cyclic ethers, vinylamines, unsaturated hydrocarbons, lactones and other cyclic esters, lactams, cyclic carbonates, cyclic acetals, aldehydes, cyclic amines, cyclic sulfides, cyclosiloxanes, and cyclotriphosphazenes.
 25. The composition as defined by claim 17, wherein said at least one polymerizable or crosslinkable oligomer belongs to at least one of the following groups: cycloaliphatic epoxies (A), non-cycloaliphatic epoxies (B), linear or cyclic alkenyl ethers (C) and mixtures of (A), (B), and/or (C) with at least one acrylic compound (D). 